Turkfleks %0.9 Sodium Chloride
NDC Package 85160-200-40

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

Turkfleks %0.9 Sodium Chloride is the solution is contraindicated in patients with hypernatremia or hyperchloremia. Marketed by Turk Ilac Ve Serum Sanayi Anonim Sirketi, this product is identified by NDC 85160-200.

Identification & Billing

NDC Package Code
85160-200-40
Package Description
25 BAG in 1 BOX / 250 mL in 1 BAG (85160-200-04)
Product Code
85160-200
11-Digit Billing Format
85160020040
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Turkfleks %0.9 Sodium Chloride
Dosage Form
-
Usage Information
The solution is contraindicated in patients with hypernatremia or hyperchloremia. It should also not be used in cases where sodium or chloride administration is clinically harmful.

Regulatory & Marketing

Labeler Name
Turk Ilac Ve Serum Sanayi Anonim Sirketi
Marketing Category
UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE -
Start Marketing Date
01-15-2025
Listing Expiration
12-31-2026
Exclude Flag
E
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (85160-200). Click a package code to view its specific billing and regulatory data.

85160-200-10
100 BAG in 1 BOX / 50 mL in 1 BAG (85160-200-01)
85160-200-20
50 BAG in 1 BOX / 100 mL in 1 BAG (85160-200-02)
85160-200-30
50 BAG in 1 BOX / 150 mL in 1 BAG (85160-200-03)
85160-200-50
20 BAG in 1 BOX / 500 mL in 1 BAG (85160-200-05)
85160-200-60
20 BAG in 1 BOX / 1000 mL in 1 BAG (85160-200-06)
85160-200-70
10 BAG in 1 BOX / 3000 mL in 1 BAG (85160-200-07)

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 85160-200-40 identifies a specific commercial package of 25 bag in 1 box / 250 ml in 1 bag (85160-200-04) of Turkfleks %0.9 Sodium Chloride, labeled by Turk Ilac Ve Serum Sanayi Anonim Sirketi. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Turk Ilac Ve Serum Sanayi Anonim Sirketi on January 15, 2025. The current certification is valid through December 31, 2026.

How is this Turk Ilac Ve Serum Sanayi Anonim Sirketi product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85160020040. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
85160-200-40
11-Digit CMS (5-4-2)
85160-0200-40

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.